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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9756Erstellt: 23. Oktober 2026

Acetic Acid → Terephthalic Acid

https://huagongshe.com/de/reaction/9756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktWaterHCID 962—
EduktP-XyleneHCID 7809—
Edukt1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trioneHCID 10419723—
KatalysatorCobalt diacetateHCID 6277—
KatalysatorManganous AcetateHCID 12525—
ProduktTerephthalic AcidHCID 748999%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

In an autoclave, 0.212 g of p-xylene, 0.011 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (3% by mole relative to p-xylene), 5 g of acetic acid, 0.003 g of cobalt(II) acetate.4H2O, 0.003 g of manganese(II) acetate.4H2O and 0.001 g of zirconium oxyacetate were placed. The autoclave was charged with 2 MPa of air and placed in a heated oil bath. The mixture was stirred at 150° C. for 12 hours. After the completion of reaction, the autoclave was placed on cold water to cool down the reaction mixture quickly. The resulting mixture was analyzed by high performance liquid chromatography and was found to yield terephthalic acid in 99% yield at 100% conversion of p-xylene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091342B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-6126e02d02c2469fb6ad8fa1a7eee34a
Quellennotizuspto-grants-2006_08